Method for the crystallization of 2-(4-N,N-diethyl amino-2-hydroxy-benzoyl)-benzoic acid-n-hexyl ester

ABSTRACT

The present invention relates to a method for the crystallization of n-hexyl 2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoate, to a method for the production of pourable or flowable particles of crystalline n-hexyl 2-(4-N,N-diethylamino-2-hydroxybenzoyl)-benzoate and to specific pourable or flowable particles of crystalline n-hexyl 2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoate.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a divisional application of U.S. application Ser.No. 12/598,227 filed Oct. 30, 2009. U.S. application Ser. No. 12/598,227is a national stage application (under 35 U.S.C. §371) ofPCT/EP2008/054645, filed Apr. 17, 2008, which claims benefit of Europeanapplication 07107342.3, filed May 2, 2007. The above applications areincorporated by reference in their entirety.

BACKGROUND OF THE INVENTION

The present invention relates to a method for the crystallization ofn-hexyl 2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoate, to a method forthe production of pourable or flowable particles of crystalline n-hexyl2-(4-N,N-diethylamino-2-hydroxy-benzoyl)benzoate and to specificpourable or flowable particles of crystalline n-hexyl2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoate.

The effects of sunlight, in particular of UV-B and of UV-A radiation, onthe human skin and the skin reactions resulting therefrom, and theoptions for protecting the skin are for the most part already known andare further investigated in detail (Chemie in unserer Zeit, 2004, 38,98-112).

Whereas UV-B radiation (290-320 nm) in particular is responsible for theformation of sunburn, UV-A radiation leads to so-called premature skinaging as a result of damage to the collagen and elastin fibers.Furthermore, UV-A radiation is able to damage DNA, which in the worstcase scenario can lead to skin cancer.

The industry therefore supplies both so-called UV-B filters and UV-Afilters in order to reduce the harmful effects of solar radiation on thehuman skin.

EP-A-1 046 391 describes the use of amino-substitutedhydroxybenzophenones as photostable UV-A filters in cosmeticpreparations.

WO 03/097578 describes a method for the production of n-hexyl2-(4-N,N-diethyl-amino-2-hydroxybenzoyl)benzoate of the formula I

where the pink-colored crude product produced in the synthesis incrystalline form from solution is firstly purified by chromatography andthen freed from the solvents present by distillation. Finally, the cleanend product is bottled as melt.

n-Hexyl 2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoate is marketedcommercially by BASF Aktiengesellschaft under the trade name Uvinul® APlus as UV-A filter. Since the product is bottled as melt and firstcrystal growth occurs after storage for about six weeks at roomtemperature, the user has to heat the entire pack to a temperature abovethe melting point of n-hexyl2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoate in order then to be ableto remove liquid product from the pack.

WO 2005/025529 describes a pulverulent preparation of n-hexyl2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoate (Uvinul® A Plus), wherethe UV-A filter is embedded in modified starch as protective colloid.The dry powder can be redispersed again in water, in which case the UV-Afilter is present in colloidally disperse form. The protective colloidhas to be tolerated in subsequent applications.

BRIEF SUMMARY OF THE INVENTION

It was an object of the present invention to provide a simple andcost-effective method for the crystallization of n-hexyl2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoate, as well an efficientmethod for the production of pourable or flowable particles ofcrystalline n-hexyl 2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoate.Furthermore, the aim was to provide a form of crystalline n-hexyl2-(4-N,N-diethylamino-2-hydroxy-benzoyl)benzoate which is safe and easyto handle by the processor.

This object is achieved by a method for the crystallization of n-hexyl2-(4-N,N-diethyl-amino-2-hydroxybenzoyl)benzoate, comprising the processsteps

a) providing a clear melt of n-hexyl2-(4-N,N-diethylamino-2-hydroxybenzoyl)-benzoate at a temperature above57° C., and

b) crystallizing out n-hexyl2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoate at a temperature below57° C.,

wherein the clear melt from process step a) is stirred at a temperaturebelow 57° C. until opacity arises, before process step b) is carriedout.

DETAILED DESCRIPTION OF THE INVENTION

On account of the origin of the n-hexyl2-(4-N,N-diethylamino-2-hydroxybenzoyl)-benzoate, it may also comprisesmall amounts of impurities from the synthesis, such as startingmaterials, intermediates, by-products and/or solvents.

The content of n-hexyl 2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoatein the melt provided in process step a) is preferably at least 90% byweight, particularly preferably at least 95% by weight, in particular atleast 98% by weight.

Accordingly, preference is given to a method according to the inventionin which the melt of n-hexyl2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoate in process step a) has apurity of at least 98% by weight, preferably at least 98.5% by weight,in particular at least 99% by weight.

Since n-hexyl 2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoate melts atabout 57° C., it suffices in principle to subject the solid startingmaterial to a temperature of only a little above 57° C. Usually, a clearmelt is provided at a temperature of from 57 to 80° C., preferably from58 to 65° C., in particular from 59 to 62° C.

Since the crystallization of n-hexyl2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoate does not startspontaneously at the melting point of the compound at 57° C., asdescribed at the start, a thermodynamically metastable melt is formedbelow the melting point, for example at room temperature.

In process step b) of the method according to the invention, n-hexyl2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoate crystallizes out at atemperature below 57° C. by stirring the clear melt from process step a)at a temperature below 57° C. until opacity arises, before process stepb) is carried out. Preferably, the melt produced in process step a) isstirred at a temperature between 25 and 40° C., particularly preferablyat a temperature between 27 and 35° C. until opaque.

For stirring the melt below 57° C., any type of stirrer can in principlebe used, such as, for example, a magnetic stirrer core, an anchorstirrer, a propeller stirrer, an oblique-blade stirrer or a diskstirrer. The size of the stirrer relative to the volume of the melt isfundamentally not decisive. Preferably, the stirrer homogenizes theentire melt during the stirring time, particularly if the melt istransferred in portions to different vessels for crystallization.

It has been established that the time until opacity arises in the melt,which is caused by the formation of crystal germs, can be reduced if thespeed of the stirrer, i.e. the number of revolutions of the stirrer pertime unit, is increased. In the method according to the invention, themelt is preferably stirred with a stirrer at a speed of from 100 to 600rpm, particularly preferably at a speed of from 200 to 500 rpm.

In the method according to the invention, the melt is preferably stirredwith a stirrer, in particular a propeller stirrer, which has a diameterof from 2 to 20 cm, at 200 to 500 rpm, in particular 300 to 400 rpm.

In the method according to the invention for the crystallization ofn-hexyl 2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoate, process step b)is preferably carried out without stirring since the melt solidifying asa result of crystallization can in any case no longer be stirred after acertain time. Therefore, after opacity has arisen, the still liquid meltcan be transferred to a desired mold, where the crystallizing out stepthen takes place. In principle, the geometry and the construction of themold are insignificant. However, preference is given to using thosemolds for which removal of the solid, crystallized-out ester presents nodifficulties. Conical molds have proven to be advantageous. The volumeof the molds is in principle arbitrary and can vary, for example, from0.1 ml to 10 l or else 5 l to 100 l. The product removed from the moldcan in turn be further comminuted in suitable devices, such as, forexample, a mill.

In the method according to the invention, in process step b), a planesurface can also be used as mold onto which the still liquid melt of theester is applied as a thin layer, i.e. with a small thickness comparedto the length-width expansion, preferably between 0.1 and 5 mm inthickness, in particular between 0.2 and 2 mm in thickness.Alternatively, the still liquid melt can also be portioned into smalldrops and be placed onto the flat surface such that so-called pastillesor prills, hemispherical structures, are formed. The diameter of thehemispheres is preferably between 0.1 and 5 mm. After the ester hascrystallized out, the solid layer or the solid pastilles or prills areremoved from the plane as is customary and bottled, the thin layersusually being comminuted to a desired flake size by breakage. Theproduction process of flakes, pastilles and prills can take placediscontinuously (batch process) or continuously, where, in a continuousmethod, a continuously circulating steel belt, for example, can be usedas mold for the purposes of the present invention.

The present invention further provides a method for the production ofpourable or flowable particles of crystalline n-hexyl2-(4-N,N-diethylamino-2-hydroxy-benzoyl)benzoate having an averageparticle diameter of from 10 μm to 22 cm, comprising the steps

a′) providing a clear melt of n-hexyl2-(4-N,N-diethylamino-2-hydroxybenzoyl)-benzoate at a temperature above57° C.,

b′) stirring the melt from process step a′) at a temperature below 57°C. until opacity arises,

c′) transferring the opaque melt to a mold,

d′) crystallizing out the transferred melt of n-hexyl2-(4-N,N-diethylamino-2-hydroxy-benzoyl)benzoate at a temperature below57° C. in the mold,

e′) removing the crystallized-out n-hexyl2-(4-N,N-diethylamino-2-hydroxy-benzoyl)benzoate from the mold andoptionally

f′) comminuting the crystalline n-hexyl2-(4-N,N-diethylamino-2-hydroxy-benzoyl)benzoate from process step e′)to the desired particle size.

By the method according to the invention it is possible to producepourable or flowable particles of crystalline n-hexyl2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoate with an average particlediameter of from 10 μm to 22 cm.

The size of the particles can be adjusted as required through the choiceof mold into which the opaque melt is transferred, or through a furthercomminution step. Preferably, particles of crystalline n-hexyl2-(4-N,N-diethylamino-2-hydroxy-benzoyl)benzoate with an averageparticle diameter of from 0.1 to 5 mm are produced by the methodaccording to the invention.

As already described above, the n-hexyl2-(4-N,N-diethylamino-2-hydroxy-benzoyl)benzoate can, owing to itsorigin, also comprise small amounts of impurities from the synthesis,such as starting materials, intermediates, by-products and/or solvents.

The content of n-hexyl 2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoatein the melt provided in process step a′) is preferably at least 90% byweight, particularly preferably at least 95% by weight, in particular atleast 98% by weight.

Accordingly, preference is given to a method according to the inventionin which the melt of n-hexyl2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoate in process step a′) hasa purity of at least 98% by weight, preferably at least 98.5% by weight,in particular at least 99% by weight.

In process step b′) of the method according to the invention, the meltfrom process step a′) is stirred at a temperature below 57° C. untilopacity arises. Preferably, process step b′) is carried out at atemperature between 25 and 40° C., particularly preferably at atemperature between 27 and 35° C.

With regard to the stirrers and stirring conditions that can be used inprocess step b′), and also preferred embodiments, reference is made tothe statements above.

The opacity which arises can be perceived visually by close inspectionor else also be ascertained by means of one or more suitable measuringcells located in the melt. It has also been established that theappearance of the opacity is accompanied by a slowing in the coolingrate as far as a slight temperature increase without input of externalenergy caused by the release of heat of crystallization. In theexperiments, it was found that upon reaching such a temperature state ofthe melt, the latter was opaque, could still be transferred withoutproblems to a mold and then, at the latest after 2 days, was completelycrystallized through.

In process step c′), the opaque melt is transferred to a mold, where inprinciple the geometry and the construction of the mold are unimportant.However, preference is given to using those molds for which removal ofthe solid, crystallized-out ester presents no difficulties. Conicalmolds have proven to be advantageous. The volume of the molds is inprinciple arbitrary and can vary, for example, from 0.1 ml to 10 l orelse 5 l to 100 l. The plane surfaces described above are likewiseadvantageous as mold from which the ester can likewise be separated offwithout problems after it has crystallized out.

In process step d′), the melt of n-hexyl2-(4-N,N-diethylamino-2-hydroxybenzoyl)-benzoate transferred to the moldor placed onto the plane surface as mold is left to crystallize out at atemperature below 57° C. Preferably, the melt is left to crystallize outat a temperature of from 15 to 35° C.

In process step e′), the crystallized-out n-hexyl2-(4-N,N-diethylamino-2-hydroxy-benzoyl)benzoate is removed from themold and optionally the crystalline n-hexyl2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoate is comminuted to thedesired particle size. Preference is given to a method in which thesolidified product from process step e′) is comminuted, preferably to anaverage particle size of from 0.1 to 5 mm. If, in process step c′), aplane surface has been used as mold for the purposes of the presentinvention, for example a steel belt, then the product which is producedin layers can, following separation from the plane surface, becomminuted by breakage, whereas the product which is produced directlyin the desired size as pastilles or prills is usually not furthercomminuted following separation from the plane surface.

The comminution step f′) can be carried out by various means or insuitable devices. Preferably, the comminution step is carried out in amill, the choice of mill being governed by the desired degree ofcomminution.

The present invention further provides pourable or flowable particles ofcrystalline n-hexyl 2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoatehaving an average particle diameter of from 0.1 to 5 mm, a bulk densitygreater than 0.35 g/ml, preferably greater than 0.4 g/ml, in particulargreater than 0.5 g/ml and a purity of at least 98% by weight, preferablyat least 98.5% by weight, in particular of at least 99% by weight.

The present invention also relates to the use of the above-describedpourable or flowable particles of crystalline n-hexyl2-(4-N,N-diethylamino-2-hydroxybenzoyl)-benzoate with an averageparticle diameter of from 0.1 to 5 mm, a bulk density greater than 0.35g/ml, preferably greater than 0.4 g/ml, in particular greater than 0.5g/ml and a purity of at least 98% by weight, preferably at least 98.5%by weight, in particular of at least 99% by weight, as UV filter or asfree-radical scavenger in cosmetic and dermatological preparations or asproduct protection.

The advantage of the method according to the invention is based on thefact that it is possible to produce the crystalline n-hexyl2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoate in a reproducible andtime-saving manner starting from a metastable melt of the high-purityester. The pourable or flowable particles of crystalline n-hexyl2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoate according to theinvention represent a nondusting form of the ester which can beincorporated without problems into cosmetic preparations.

The invention is explained by the following, but non-invention-limitingexamples.

The melting point of the n-hexyl2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoate used was measured inaccordance with Ph. Eur. (European Pharmacopoeia 5.0). A value of 57° C.was determined as melting point.

Experiments for Controlled Crystallization Example 1 Comparative Example

5 kg of molten n-hexyl 2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoatewith a purity of more than 99% were allowed to cool at room temperatureand stand in order to achieve crystallization of the substance. Firstcrystals were observed after 10 days. After 2 months, the entire mass ofthe ester had crystallized.

Example 2 Comparative Example

At about 40° C., 100 g of fine crystals of n-hexyl2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoate (<100 μm) were added to5 kg of molten n-hexyl 2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoate.The melt was then left to cool to room temperature. First crystals wereobserved after 10 days. After 2 months, the entire mass of the ester hadcrystallized.

Example 3 Comparative Example

5 kg of molten n-hexyl 2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoatewas allowed to cool to 5° C. and stand at this temperature in order toachieve crystallization of the substance. First crystals were observedafter 10 days. After 2 months at 5° C., the entire mass of the ester hadcrystallized.

Example 4 Comparative Example

At about 40° C., 100 g of fine crystals of n-hexyl2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoate (<100 μm) were added to5 kg of molten n-hexyl 2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoate.The melt was then left to cool to room temperature. First crystals wereobserved after 10 days. After 2 months, the entire mass of the ester hadcrystallized.

Example 5 According to the Invention

5 kg of molten n-hexyl 2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoatewere transferred to a 5 l aluminum container. Using a magnetic stirrerrod (40 mm), the melt, cooling to room temeprature, was stirred for 4hours at 80 rpm. After 4 hours, first crystals were observed. Completecrystallization took place within 14 days.

Example 6 According to the Invention

5 kg of molten n-hexyl 2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoatewere transferred to a 5 l aluminum container. The melt was stirred witha PTFE propeller stirrer (60 mm diameter), which was driven by anelectric motor at a stirring speed of 250 rpm at room temperature. Afterthe melt had been stirred for 11 hours, the viscosity of the melt hadincreased so much that stirring could not be continued. First crystalsappeared after stirring for five hours and complete crystallization tookplace within 24 hours.

Example 7 According to the Invention

800 g of molten n-hexyl 2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoatewere transferred to a 1 l glass jacketed reactor (HWS). The temperatureof the melt was 60° C. The melt was stirred using a PTFE blade stirrer(75 mm diameter) for 6 hours with a stirring speed of 350 rpm. Firstcrystals were observed after 4 hours and the temperature of the melt atthis time was about 33° C. This temperature of the melt remainedconstant for some time. After 6 hours, a very opaque melt was observed,the temperature of which was 33° C. This opaque, viscous melt wastransferred from the reactor to an aluminum crystallization container.Complete crystallization took place within 24 hours.

Example 8 According to the Invention

800 g of molten n-hexyl 2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoatewere transferred to a 1 l glass jacketed reactor (HWS), and the melt wasstirred using a PTFE blade stirrer (75 mm diameter) with a stirringspeed of 250 rpm. After 2 hours, the melt had a temperature, whichremained constant, of 28° C. The cloud point of the melt was achievedafter stirring for twelve hours. Complete crystallization of the estertook place within 24 hours.

Example 9 According to the Invention

1000 g of molten n-hexyl 2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoatewere transferred, as 60° C. warm melt, to a 1 l glass jacketed reactor(HWS). The melt cooled without stirring over the course of 2 hours to atemperature of 32° C. The melt was then stored for 18 hours withoutstirring and themostated at 35° C. The thermostating was switched offand the melt was stirred using a PTFE propeller stirrer (60 mm diameter)for 30 minutes at a stirring speed of 350 rpm. After stirring for tenminutes, the temperature of the melt was 33° C. After stirring forthirty minutes, the temperature of the melt was 33.5° C. The melt becameopaque and first crystals were evident. The melt was then transferred toan aluminum mold. Complete crystallization of the ester took placewithin 4 hours.

Experiments for Grinding Example 10 According to the Invention

100 g of crystalline n-hexyl2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoate from example 9 werecomminuted in an attrition mill (Alexander grater in food mode with a3-blade rotor from Alexanderwerk Remscheid) with a sieve of mesh width4.0×7.5 mm, 71.2% of the comminuted material had a particle size in therange of from 0.5 to 5 mm. The fines fraction with a particle size ofless than 100 μm had a content of 2.5% by weight. This fines fractionwas determined by sieving.

The invention claimed is:
 1. A pourable or flowable particle ofcrystalline n-hexyl 2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoate withan average particle diameter of from 0.1 to 5 mm, a bulk density greaterthan 0.35 g/ml and a purity of at least 98% by weight.
 2. The pourableor flowable particle as claimed in claim 1, wherein the purity is atleast 99% by weight.
 3. The pourable or flowable particle as claimed inclaim 1, wherein the bulk density is greater than 0.5 g/ml.
 4. Thepourable or flowable particle as claimed in claim 2, wherein the bulkdensity is greater than 0.5 g/ml.
 5. An article which comprisesutilizing the pourable or flowable particle as claimed in claim 1wherein the article is a UV filter, free-radical scavenger in cosmeticand dermatological preparation or a product protection.
 6. An articlewhich comprises utilizing the pourable or flowable particle as claimedin claim 4 wherein the article is a UV filter, free-radical scavenger incosmetic and dermatological preparation or a product protection.
 7. Thepourable or flowable particle as claimed in claim 1, wherein the purityis at least 98.5% by weight.
 8. The pourable or flowable particle asclaimed in claim 1, wherein the bulk density is greater than 0.4 g/ml.9. The pourable or flowable particle as claimed in claim 1, wherein theaverage particle diameter of from 0.5 to 5 mm.
 10. The pourable orflowable particle as claimed in claim 4, wherein the average particlediameter of from 0.5 to 5 mm.
 11. The pourable or flowable particle asclaimed in claim 1, wherein said n-hexyl2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoate is made comprising thesteps a) providing a clear melt of n-hexyl2-(4-N,N-diethylamino-2-hydroxybenzoyl)-benzoate at a temperature above57° C., and b) crystallizing out n-hexyl2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoate at a temperature below57° C., wherein the clear melt from process step a) is stirred at atemperature below 57° C. until opacity arises, before process step b) iscarried out.
 12. The pourable or flowable particle as claimed in claim10, wherein said n-hexyl 2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoateis made comprising the steps a) providing a clear melt of n-hexyl2-(4-N,N-diethylamino-2-hydroxybenzoyl)-benzoate at a temperature above57° C., and b) crystallizing out n-hexyl2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoate at a temperature below57° C., wherein the clear melt from process step a) is stirred at atemperature below 57° C. until opacity arises, before process step b) iscarried out.
 13. The pourable or flowable particle as claimed in claim1, wherein b) crystallizing out n-hexyl2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoate at a temperature from 25to 40° C.
 14. The pourable or flowable particle as claimed in claim 1,wherein b) crystallizing out n-hexyl2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoate at a temperature from 27to 35° C.
 15. The pourable or flowable particle as claimed in claim 12,wherein b) crystallizing out n-hexyl2-(4-N,N-diethylamino-2-hydroxybenzoyl)benzoate at a temperature from 27to 35° C.